Enoxolone

Enoxolone

Catalog Number:
FC01365904APE
Mfr. No.:
APE-B5986
Price:
$180
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          Background

          Glycyrrhetinic acid (enoxolone) is a major component of a plant called licorice. It has been found to have both antiviral and antifungal activities. It is able to carboxilate the replication of DNA and inhibits the production of microbial toxins and enzymes [1] [2]. In rats, 18β-Glycyrrhetinic acid potently inhibited 11β-hydroxysteroid dehydrogenase (11β-HSD) activity of hepatic and renal homogenates with IC50 values of 0.09 μm and 0.36 μm, respectively [3].Before glucocorticoids bind the mineralocorticoid receptor (MR), the selectivity of MR for aldosterone can be exerted by enzymes, and hence competing glucocorticoids is inactivated. 11β-HSD-1 and 11β-HSD-2 and 11β-HSD-3 are three of the enzymes. 11β-HSD-1 has bidirectional activity and a Km value in the micromolar range. It is NADP+-dependent. 11β-HSD-2 exhibits only oxidase activity and has a Km in the nanomolar range. It is NAD+-dependent. In the kidney, it colocalizes with the MR [4].JEG-3 cell line was derived from a human choriocarcinoma. In this cell line, the enzyme activity of 11β-HSD-3 was inhibited by glycyrrhetinic acid [4].In rats, 3 h after the administration of glycyrrhetinic acid at concentration of 200 mg/kg, p.o. significantly inhibited 11β-HSD activity in the kidney and the liver. In addition, glycyrrhetinic acid slightly increased the circulating corticosterone level. In differential inhibitory effects on 11β-HSD isozyme activity, the 11-, 24- and 30-positions of glycyrrhetinic acid may play important roles. This had been showed by Data [3].

          [1]. Salari MH, Sohrabi N, Kadkhoda Z, et al. Antibacterial Effects of Enoxolone on Periodontopathogenic and Capnophilic Bacteria Isolated from Specimens of Periodontitis Patients. Iranian Biomedical Journal, 2003, 7(1):39-42.
          [2]. Bahmani M, Rafieian-Kopaei M, Jeloudari M, et al. A review of the health effects and uses of drugs of plant licorice (Glycyrrhiza glabra L.) in Iran. Asian Pacific Journal of Tropical Disease, 2015, 5: 127-29.
          [3]. Shimoyama Y, Hirabayashi K, Matsumoto H, et al. Effects of glycyrrhetinic acid derivatives on hepatic and renal 11beta-hydroxysteroid dehydrogenase activities in rats. J Pharm Pharmacol, 2003, 55(6):811-7.
          [4]. Gomez-Sanchez EP, Cox D, Foecking M, et al. 11 beta-hydroxysteroid dehydrogenases of the choriocarcinoma cell line JEG-3 and their inhibition by glycyrrhetinic acid and other natural substances. Steroids, 1996, 61(3):110-5.

      • Properties
        • Categories
          major component of licorice
          Alternative Name
          (2S,4aS,6aS,6bR,8aR,10S,12aS,12bR,14bR)-10-hydroxy-2,4a,6a,6b,9,9,12a-heptamethyl-13-oxo-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-2-carboxylic acid
          CAS Number
          471-53-4
          Molecular Formula
          C30H46O4
          Molecular Weight
          470.68
          Appearance
          A solid
          Purity
          99.12%
          Solubility
          insoluble in H2O; ≥19.3 mg/mL in DMSO; ≥26.5 mg/mL in EtOH
          Storage
          Store at -20°C
          SMILES
          CC([[email protected]]1([H])CC[[email protected]]23C)([[email protected]](O)([H])CC[[email protected]@]1([[email protected]@]2([H])C(C=C4[[email protected]]5([H])C[[email protected]](CC[[email protected]](CC[[email protected]]43C)5C)(C(O)=O)C)=O)C)C

          * For Research Use Only

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